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1208

by Siam intermagnate CO., LTD.

Ref 1208Model Patient waste containers

1208 is a Class I device made by Siam intermagnate CO., LTD., registered in EUDAMED on 15 Apr 2025 (Basic UDI-DI 885642200003GM), active as of 22 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number885642200003GM Basic UDI-DI 08856422002311UDI-DIDate15 Apr 2025RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Patient waste containers, 1208
Primary DI / UDI-DI
08856422002311
Basic UDI-DI
885642200003GM
EMDN code
V0480 Clinical use containers (non-IVD) - accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
TH-MF-000003828
Authorised representative
Advena Limited MT-AR-000000234

Related devices

Category: Surgical instrument/implant rack

Other devices from Siam intermagnate CO., LTD.

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Properties

  • Sterilise before use
Other properties (13, all answered No)